TINTED FACE CREAM SPF 15- octocrylene, octisalate cream

Tinted Face Cream by

Drug Labeling and Warnings

Tinted Face Cream by is a Otc medication manufactured, distributed, or labeled by Bentley Laboratories, LLC, Geologie. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

DRUG FACTS

Active Ingredients

Octocrylene 5%

Octisalate 2%

PURPOSE

Purpose

Octocrylene ....... Sunscreen

Octisalate .......... Sunscreen

INDICATIONS & USAGE

Uses Helps prevent sunburn if used as directed with other sun protection measures (see Directions) decreases the
risk of skin cancer and early signs of skin aging from the sun.

WARNINGS

Warnings For external use only.  Do not use on damaged or broken skin.  When using this product keep

out of eyes. Rinse with water to remove. Stop use and ask doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children. If swallowed get medical help

or contact a Poison Control center right away.

DOSAGE & ADMINISTRATION

Directions  ​​ Use in the morning.  Rub evenly into your entire face and neck, avoiding the eyes.

INACTIVE INGREDIENT

Inactive IngredientsAloe Barbadensis Leaf Juice, Water, Butyloctyl Salicylate, Cetear-
yl Olivate, Sorbitan Olivate, Glyceryl Stearate, Potassium Azeloyl Diglycinate, Glycerin, Niacina-
mide, Polyglyceryl-10 Laurate, Sodium Hyaluronate, Silica, Caffeine, Phenoxyethanol, Caprylyl
Glycol, Dimethicone, Sodium Stearoyl Glutamate, Hydroxyethyl Acrylate/Sodium Acryloyldi-
methyl Taurate Copolymer, Ethyl Ferulate, Ethylhexylglycerin, Arnica Montana Flower Extract

Geologie Moisturizing Morning Cream SPF 15 Tinted Labeling

PERSONALIZED SKINCARE

Moisturizing Morning Cream
SPF 15 TINTED

Geologie.com
Made in USA of
Imported Materials
Distributed by Geologie
New York, NY 10025

20 mL Tube

60 mL Tube

res

INGREDIENTS AND APPEARANCE

TINTED FACE CREAM  SPF 15
octocrylene, octisalate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54111-186
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	5.0 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	OCTISALATE	2.0 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE BARBADENSIS LEAF JUICE POWDER (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
SORBITAN OLIVATE (UNII: MDL271E3GR)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
POTASSIUM AZELOYL DIGLYCINATE (UNII: N02RVN6NYP)
GLYCERIN (UNII: PDC6A3C0OX)
NIACINAMIDE (UNII: 25X51I8RD4)
POLYGLYCERYL-10 LAURATE (UNII: MPJ2Q8WI8G)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
SILICA (UNII: ETJ7Z6XBU4)
CAFFEINE (UNII: 3G6A5W338E)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
DIMETHICONE (UNII: 92RU3N3Y1O)
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
ETHYL FERULATE (UNII: 5B8915UELW)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54111-186-20	20 mL in 1 TUBE; Type 0: Not a Combination Product	07/18/2023
2	NDC: 54111-186-60	60 mL in 1 TUBE; Type 0: Not a Combination Product	07/18/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	07/18/2023

Labeler - Bentley Laboratories, LLC (068351753)

Registrant - Geologie (081158549)